A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981837



Internal ID12974012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:93619013..93693126hg38UCSC Ensembl
Innerchr15:94162242..94236355hg19UCSC Ensembl
Innerchr15:91963246..92037359hg18UCSC Ensembl
Innerchr15:91963246..92037359hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3874114
hg1974114
hg1874114
hg1774114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751543
Supporting Variants
SamplesBEC_492
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981837
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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